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Celecoxib in Preventing Skin Cancer in Patients With Actinic Keratoses

1 de agosto de 2013 actualizado por: University of Alabama at Birmingham

A Phase II/III Randomized, Double-Blind, Placebo-Controlled Clinical Trial Of Celecoxib In Subjects With Actinic Keratoses

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. The use of celecoxib may be an effective way to prevent actinic keratoses.

PURPOSE: Randomized phase II/III trial to determine the effectiveness of celecoxib in preventing skin cancer in patients who have actinic keratoses.

Descripción general del estudio

Estado

Retirado

Intervención / Tratamiento

Descripción detallada

OBJECTIVES:

  • Compare celecoxib vs placebo in terms of preventing the development of new actinic keratoses in patients with actinic keratoses.
  • Compare these treatment regimens in terms of inducing regression of actinic keratoses in these patients.
  • Determine the safety of this drug in these patients.
  • Compare the effect of these treatment regimens on potential surrogate end-point biomarkers in areas of actinic keratosis, sun-exposed skin, and non-sun-exposed skin and correlate these biomarkers with clinical outcome in these patients.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive oral celecoxib twice daily for 9 months in the absence of disease progression or unacceptable toxicity.
  • Arm II: Patients receive oral placebo as in arm I. Patients are followed at 2 months after completing treatment.

PROJECTED ACCRUAL: A total of 240 patients (120 per treatment arm) will be accrued for this study.

Tipo de estudio

Intervencionista

Fase

  • Fase 2
  • Fase 3

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Alabama
      • Birmingham, Alabama, Estados Unidos, 35294-3300
        • University of Alabama at Birmingham Comprehensive Cancer Center
    • California
      • Irvine, California, Estados Unidos, 92697
        • Chao Family Comprehensive Cancer Center at University of California Irvine Cancer Center
    • Michigan
      • Ann Arbor, Michigan, Estados Unidos, 48109-0314
        • University Of Michigan Comprehensive Cancer Center
    • Missouri
      • Saint Louis, Missouri, Estados Unidos, 63110
        • Siteman Cancer Center at Barnes-Jewish Hospital
    • New York
      • Rochester, New York, Estados Unidos, 14642
        • James P. Wilmot Cancer Center at University of Rochester Medical Center
    • Texas
      • Houston, Texas, Estados Unidos, 77030-4009
        • University of Texas - MD Anderson Cancer Center
    • Wisconsin
      • Madison, Wisconsin, Estados Unidos, 53792-6164
        • University of Wisconsin Comprehensive Cancer Center

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

DISEASE CHARACTERISTICS:

  • Diagnosis of Fitzpatrick skin types I, II, or III
  • Sun-damaged skin with 10-40 actinic keratoses on the upper extremities (upper arms, forearms, and hands), neck, face, and scalp combined

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • Not specified

Life expectancy:

  • Not specified

Hematopoietic:

  • WBC at least 3,000/mm^3
  • Platelet count at least 125,000/mm^3
  • Hemoglobin at least lower limit of normal
  • No significant bleeding disorder

Hepatic:

  • Bilirubin no greater than 1.5 times upper limit of normal (ULN)
  • AST and ALT no greater than 1.5 times ULN
  • No chronic or acute hepatic disorder

Renal:

  • Creatinine no greater than 1.5 times ULN
  • BUN no greater than 1.5 times ULN
  • No chronic or acute renal disorder

Gastrointestinal:

  • No history of or active inflammatory bowel disease
  • No active pancreatitis
  • Not diagnosed with esophageal, gastric, pyloric channel, or duodenal ulceration within the past 30 days

Other:

  • No history of keloid formation
  • No known photosensitivity disorder
  • No history of hypersensitivity or adverse reaction to sulfonamides, COX-2 inhibitors, salicylates, or other NSAIDs
  • No other condition that would preclude study
  • No other medical or psychosocial condition that would preclude study
  • No other malignancy within the past 5 years except:

    • Carcinoma in situ of the cervix
    • Curatively excised nonmelanoma skin cancer
    • Stage 0 chronic lymphocytic leukemia
    • Any cancer for which the patient is currently without evidence of disease, has not been treated for tumor within the past 6 months, has no current or planned therapy, and has an expected disease-free survival of at least 5 years
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • At least 30 days since prior systemic immunotherapy
  • No concurrent immunotherapy

Chemotherapy:

  • At least 3 months since prior topical fluorouracil (5-FU)
  • At least 6 months since other prior topical chemotherapy
  • No concurrent topical chemotherapy, including 5-FU
  • No other concurrent chemotherapy

Endocrine therapy:

  • At least 6 months since prior oral or IV corticosteroids for more than 2 consecutive weeks
  • At least 6 months since prior inhaled or nasal corticosteroids for more than 4 weeks duration
  • At least 14 days since prior topical corticosteroids
  • At least 30 days since prior nasal corticosteroids (except mometasone)
  • No concurrent oral or IV corticosteroids for more than 2 consecutive weeks during any 6 month period during study
  • No concurrent inhaled or nasal steroids (except mometasone) for more than 4 weeks during any 6 month period during study
  • No concurrent hormonal or steroidal therapy, including topical corticosteroids
  • Concurrent hormone replacement therapy (e.g., estrogen or thyroid hormone replacement) allowed

Radiotherapy:

  • At least 6 months since prior local radiotherapy to areas being studied
  • At least 30 days since other prior radiotherapy
  • No concurrent radiotherapy, including local radiotherapy to areas being studied

Surgery:

  • Not specified

Other:

  • At least 30 days since prior cryotherapy to target lesions
  • At least 60 days since prior laser resurfacing, dermabrasion, or chemical peels
  • At least 30 days since prior investigational medication
  • At least 14 days since prior topical alphahydroxyacids (e.g., glycolic acid or lactic acid) or retinoids
  • At least 30 days since prior systemic psoralens or retinoids
  • At least 30 days since prior treatment for esophageal, gastric, pyloric channel, or duodenal ulcers
  • At least 30 days since prior aspirin (more than 100 mg/day), other nonsteroidal anti-inflammatory drugs (NSAIDs) or COX-2 inhibitors at a frequency of at least 3 times per week for more than 2 weeks (except cardioprotective doses of aspirin (no more than 100 mg/day)
  • No concurrent systemic psoralens or retinoids
  • No concurrent prescription or over-the-counter topical medications to areas being studied (e.g., vitamin A derivatives)
  • No concurrent cryotherapy to target lesions
  • No concurrent laser resurfacing, dermabrasion, or chemical peels
  • No other concurrent investigational medications
  • No concurrent fluconazole or lithium
  • No concurrent chronic NSAIDs or COX-2 inhibitors (at least 3 times per week for more than 2 consecutive weeks per year)
  • Concurrent cardioprotective doses of oral aspirin (100 mg per day or less) allowed
  • Concurrent moisturizer/emollient or sunscreen allowed

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Triple

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Group 1 active arm
receipt of active drug
Experimental: Group 2 active arm
receipt of active drug
Experimental: group 2 placebo arm
receipt of placebo

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Compare celecoxib vs placebo in terms of preventing the development of new actinic keratoses in patients with actinic keratoses.
Periodo de tiempo: baseline to 2 months after last dose
baseline to 2 months after last dose

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Compare these treatment regimens in terms of inducing regression of actinic keratoses in these patients.
Periodo de tiempo: baseline to 2 months after last dose
baseline to 2 months after last dose
Compare the effect of these treatment regimens on potential surrogate end-point biomarkers in areas of actinic keratosis, sun-exposed skin, and non-sun-exposed skin and correlate these biomarkers with clinical outcome in these patients.
Periodo de tiempo: baseline to 2 months after last dose
baseline to 2 months after last dose

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Silla de estudio: Craig A. Elmets, MD, University of Alabama at Birmingham

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de diciembre de 2001

Finalización primaria (Actual)

1 de diciembre de 2005

Finalización del estudio (Actual)

1 de diciembre de 2005

Fechas de registro del estudio

Enviado por primera vez

7 de diciembre de 2001

Primero enviado que cumplió con los criterios de control de calidad

26 de enero de 2003

Publicado por primera vez (Estimar)

27 de enero de 2003

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

5 de agosto de 2013

Última actualización enviada que cumplió con los criterios de control de calidad

1 de agosto de 2013

Última verificación

1 de noviembre de 2012

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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